BMC bioinformatics · 2026
scKSFD: federated distillation model with knowledge sharing for cell type classification of clinical transcriptome data.
СтатьяНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Sun Nan, Guan Mengcen, Zhou Piyu, Yau Stephen S-T
Аннотация
Single-cell RNA sequencing (scRNA-seq) enables high resolution characterization of cellular heterogeneity but poses significant challenges for cross institutional collaboration due to privacy constraints and distributional heterogeneity. To address this problem, we propose a Federated Distillation framework with Knowledge Sharing (scKSFD) for privacy-preserving cell type classification. Unlike conventional federated learning approaches that exchange model parameters, scKSFD performs knowledge aggregation in prediction space by sharing probability-level soft label outputs on a reference dataset, thereby reducing privacy risks. To better accommodate domain specific characteristics of scRNA-seq data, scKSFD integrates stratified proxy sampling to preserve rare cell populations and employs probability-level aggregation to mitigate batch specific expression shifts without explicit feature level correction. Comprehensive evaluations across 42 clinical single-cell transcriptome datasets demonstrate that scKSFD achieves higher or comparable F1 scores relative to centralized and existing federated baselines under heterogeneous settings, with statistically significant improvements in paired comparisons. In a multiple hospital COVID-19 case study, federated collaboration using scKSFD improved classification performance compared with local-only training while avoiding direct sharing of patient level expression data. Overall, scKSFD provides a federated distillation framework that balances predictive performance, robustness, and data-sharing constraints for multiple institutional single-cell transcriptomic analysis.